Mc Donald Darran, Goulden Eirena, Cullen Garret, Crown John, Crowley Rachel K
Department of Endocrinology, St Vincent's University Hospital, Dublin, Ireland.
Department of Gastroenterology, St Vincent's University Hospital, Dublin, Ireland.
Endocrinol Diabetes Metab Case Rep. 2021 Oct 1;2021. doi: 10.1530/EDM-21-0130.
Thyroid dysfunction is among the most common immune-related adverse reactions associated with immune checkpoint inhibitors. It most commonly manifests as painless thyroiditis followed by permanent hypothyroidism. This usually causes mild toxicity that does not interfere with oncological treatment. In rare instances, however, a life-threatening form of decompensated hypothyroidism called myxoedema coma may develop. We present a case of myxoedema coma in a woman in her sixties who was treated with a combination of CTLA-4 and PD-1 immune checkpoint inhibitors; for stage four malignant melanoma. She became hypothyroid and required thyroxine replacement after an episode of painless thyroiditis. Six months after the initial diagnosis of malignant melanoma, she presented to the emergency department with abdominal pain, profuse diarrhoea, lethargy and confusion. She was drowsy, hypotensive with a BP of 60/40 mmHg, hyponatraemic and hypoglycaemic. Thyroid function tests (TFTs) indicated profound hypothyroidism with a TSH of 19 mIU/L, and undetectable fT3 and fT4, despite the patient being compliant with thyroxine. She was diagnosed with a myxoedema coma caused by immune-related enteritis and subsequent thyroxine malabsorption. The patient was treated with i.v. triiodothyronine (T3) and methylprednisolone in the ICU. While her clinical status improved with T3 replacement, her enteritis was refractory to steroid therapy. A thyroxine absorption test confirmed persistent malabsorption. Attempts to revert to oral thyroxine were unsuccessful. Unfortunately, the patient's malignant melanoma progressed significantly and she passed away four months later. This is the first reported case of myxoedema coma that resulted from two distinct immune-related adverse reactions, namely painless thyroiditis and enterocolitis.
Myxoedema coma, a severe form of decompensated hypothyroidism is a rare immunotherapy-related endocrinopathy. Myxedema coma should be treated with either i.v. triiodothyronine (T3) or i.v. thyroxine (T4). Intravenous glucocorticoids should be co-administered with thyroid hormone replacement to avoid precipitating an adrenal crisis. Thyroid function tests (TFTs) should be monitored closely in individuals with hypothyroidism and diarrhoea due to the risk of thyroxine malabsorption. A thyroxine absorption test can be used to confirm thyroxine malabsorption in individuals with persistent hypothyroidism.
甲状腺功能障碍是与免疫检查点抑制剂相关的最常见免疫相关不良反应之一。最常见的表现为无痛性甲状腺炎,随后发展为永久性甲状腺功能减退。这通常会导致轻度毒性,不影响肿瘤治疗。然而,在罕见情况下,可能会发生一种危及生命的失代偿性甲状腺功能减退形式,称为黏液性水肿昏迷。我们报告一例黏液性水肿昏迷病例,患者为一名60多岁女性,因四期恶性黑色素瘤接受了CTLA-4和PD-1免疫检查点抑制剂联合治疗。她在经历无痛性甲状腺炎后出现甲状腺功能减退,需要甲状腺素替代治疗。在最初诊断为恶性黑色素瘤六个月后,她因腹痛、大量腹泻、嗜睡和意识模糊被送往急诊科。她嗜睡,血压低至60/40 mmHg,低钠血症且低血糖。甲状腺功能检查(TFTs)显示严重甲状腺功能减退,促甲状腺激素(TSH)为19 mIU/L,游离三碘甲状腺原氨酸(fT3)和游离甲状腺素(fT4)检测不到,尽管患者一直遵医嘱服用甲状腺素。她被诊断为由免疫相关肠炎及随后的甲状腺素吸收不良导致的黏液性水肿昏迷。患者在重症监护病房接受静脉注射三碘甲状腺原氨酸(T3)和甲泼尼龙治疗。虽然T3替代治疗使她的临床状况有所改善,但她的肠炎对类固醇治疗无效。甲状腺素吸收试验证实存在持续吸收不良。尝试恢复口服甲状腺素未成功。不幸的是,患者的恶性黑色素瘤显著进展,四个月后去世。这是首例由两种不同的免疫相关不良反应,即无痛性甲状腺炎和小肠结肠炎导致的黏液性水肿昏迷病例。
黏液性水肿昏迷是失代偿性甲状腺功能减退的一种严重形式,是一种罕见的免疫治疗相关内分泌病。黏液性水肿昏迷应使用静脉注射三碘甲状腺原氨酸(T3)或静脉注射甲状腺素(T4)进行治疗。静脉注射糖皮质激素应与甲状腺激素替代治疗同时使用,以避免引发肾上腺危象。由于存在甲状腺素吸收不良的风险,对于甲状腺功能减退且腹泻的患者,应密切监测甲状腺功能检查(TFTs)。甲状腺素吸收试验可用于确诊持续甲状腺功能减退患者的甲状腺素吸收不良。